Canonical Allele Identifier: PA1139734671
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 972221
ClinVar RCV Id: RCV001248197 RCV002418854 RCV001760287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly696Glu
CA6264927
NM_001351834.2:c.2087G>A